Dayal R, Decrind C, Lambert P H
Bull World Health Organ. 1986;64(3):403-14.
Several laboratories have reported a large number of plasmodial antigens that may be implicated in the immune-mediated protection against the asexual blood stage of Plasmodium falciparum. In order to establish relationships between the antigens reported by different laboratories, a comparative testing of 37 antibody reagents was carried out at the Reference Laboratory for Malaria Antibodies and Antigens. Based on the results of the comparative testing, these antibodies were divided into seven groups according to similarities in the stage-specificity, the subcellular localization and the apparent molecular mass (M(r)) of the antigens they recognized.Twenty-two antibody reagents were grouped together on the basis that all gave a characteristic grape-pattern in indirect immunofluorescence (IIF) and precipitated a schizont/merozoite antigen of M(r) 190 000 to 205 000. Another group consisted of one antibody which reacted with a M(r) 90 000 protein expressed only in mature trophozoites and young schizonts. A third group consisted of three antibodies which reacted with all blood stages of the parasite and recognized a M(r) 36 000 protein. The fourth group contained one antibody which recognized a M(r) 14 000 protein and gave an IIF staining of schizonts. The fifth group consisted of an antiserum raised against a fusion protein. This antiserum reacted with schizont and ring-stage parasites and precipitated a M(r) 75 000 antigen. One rabbit antiserum raised against a different fusion protein and one monoclonal antibody (Mab) were put together in the sixth group on the basis that both gave a cytoplasmic IIF staining of schizonts and recognized a strain-specific, M(r) 250 000 antigen from one P. falciparum strain. A seventh group was made up of 8 antibodies on the basis that all gave a similar two-dot IIF staining pattern of segmented schizonts and free merozoites, although these antibodies recognized four different sets of antigens.These results were presented to a subcommittee of the Scientific Working Group on the Immunology of Malaria (SWG-IMMAL) during a workshop held at the reference laboratory. The P. falciparum proteins recognized by the antibody reagents used for this workshop represent only some of the different types of asexual blood-stage antigens that have been described in the literature..
几个实验室报告了大量可能与免疫介导的针对恶性疟原虫无性血液阶段的保护作用有关的疟原虫抗原。为了建立不同实验室报告的抗原之间的关系,疟疾抗体和抗原参考实验室对37种抗体试剂进行了对比检测。根据对比检测结果,这些抗体根据它们识别的抗原在阶段特异性、亚细胞定位和表观分子量(M(r))方面的相似性被分为七组。22种抗体试剂被归为一组,因为它们在间接免疫荧光(IIF)中都呈现出特征性的葡萄样图案,并沉淀出分子量为190000至205000的裂殖体/裂殖子抗原。另一组由一种抗体组成,它与仅在成熟滋养体和年轻裂殖体中表达的分子量为90000的蛋白质发生反应。第三组由三种抗体组成,它们与寄生虫的所有血液阶段发生反应,并识别出一种分子量为36000的蛋白质。第四组包含一种抗体,它识别一种分子量为14000的蛋白质,并对裂殖体进行IIF染色。第五组由针对融合蛋白产生的抗血清组成。这种抗血清与裂殖体和环状阶段寄生虫发生反应,并沉淀出一种分子量为75000的抗原。一种针对不同融合蛋白产生的兔抗血清和一种单克隆抗体(Mab)被归为第六组,因为它们都对裂殖体进行细胞质IIF染色,并识别来自一株恶性疟原虫的菌株特异性、分子量为250000的抗原。第七组由8种抗体组成,因为它们对分段裂殖体和游离裂殖子都呈现出相似的两点IIF染色模式,尽管这些抗体识别四组不同的抗原。在参考实验室举办的一次研讨会上,这些结果提交给了疟疾免疫学科学工作组(SWG-IMMAL)的一个小组委员会。用于本次研讨会的抗体试剂所识别的恶性疟原虫蛋白质仅代表文献中描述的一些不同类型的无性血液阶段抗原。